Advances in Materials Science and Engineering

Advances in Materials Science and Engineering / 2016 / Article

Research Article | Open Access

Volume 2016 |Article ID 5819208 |

Bronislaw Buczek, "Preparation of Active Carbon by Additional Activation with Potassium Hydroxide and Characterization of Their Properties", Advances in Materials Science and Engineering, vol. 2016, Article ID 5819208, 4 pages, 2016.

Preparation of Active Carbon by Additional Activation with Potassium Hydroxide and Characterization of Their Properties

Academic Editor: Jainagesh A. Sekhar
Received15 Nov 2015
Revised08 Jan 2016
Accepted10 Jan 2016
Published24 Jan 2016


A commercially available activated carbon was used to prepare active carbon via reactivation with KOH at 750°C. Active carbon was obtained with 60.5% yield. The resulting active carbon showed a well-developed porous structure with specific surface area 2939 m2/g, total pore volume 1.488 cm3/g, and micropore volume 1.001 cm3/g. Process reactivation of carbon changes its particle size as well as density properties and increases by nearly twice the amounts of methane and carbon dioxide adsorbed under high pressure conditions. Such active carbon may be used to enrich methane or carbon dioxide by pressure swing adsorption technique. Other possible applications of reactivated carbon are storage of hydrogen and methane and sequestration of carbon dioxide.

1. Introduction

Activated carbons are produced from different precursors, such as wood, peat, brown coal, lignite, various types of hard coal, anthracite, carbo- and petrochemical products, polymers, and fruit shells [1, 2]. Typically, all organic precursor can be converted into activated carbons; however, in most cases, it requires the usage of an activation agent and only a few are commercially attractive. The properties of the final product depend on the nature of raw material used, the nature of activating agent, and the conditions of activation process.

The traditional production of activated carbon consists of two steps: (i) carbonization of the precursor at a temperature below 900°C in inert atmosphere and (ii) chemical or physical chemical activation of the carbonized precursor [3].

In the chemical activation process, either the previously carbonized product is impregnated with suitable chemical agents, such as acids (HNO3, H2SO4, and H3PO4) or salts (ZnCl2, MgCl2, FeCl3, AlCl3, and K2S). These reagents act by solubilized cellulose, which, at elevated temperatures, separates, as a highly dispersed amorphous carbon, which forms a porous structure in the carbonaceous adsorbent.

When the chemical treatment is carried out with sulphuric acid at temperatures <200°C, the active carbon shows poor sorption capabilities. During activation with phosphoric acid at 375–500°C, corrosion problems appear with the equipment. One drawback of activation with zinc chloride at 550–650°C is that the active carbon is polluted with zinc salts, which are difficult to remove.

Amoco Corporation developed a process to produce high surface area carbons (over 3000 m2/g) by the KOH activation of aromatic precursors such petroleum coke and coal. The process was commercialized in the 1980s and was subsequently licensed and operated on pilot plant by the Kansai Coke and Chemicals Co. At this time, only limited quantities of products have been produced. The activated carbon is predominantly microporous, which is responsible for high surface area, and the total pore volume is exceptionally high: 2.0–2.6 mL/g [4].

Increasing interest in activation with potassium hydroxide from such precursors as wood and vegetable shells has led to investigations of the chemistry and mechanism of formation of activated carbon with a perfectly developed porous structure and a very high specific surface area [5].

The paper presents the results of studies on increasing the adsorption capacity of a commercial active carbon for methane and carbon dioxide by additional activation with potassium hydroxide.

2. Experimental

2.1. Material and Reactivation with KOH

The material for the additional chemical treatment was Picazine active carbon [6] manufactured from pinewood by Société PICA, France. The original chemical activation was done using orthophosphoric acid.

2.1.1. Reactivation of Active Carbon

Picazine carbon was dried and then mixed with ground KOH in the ratio 1 : 3 (m/m). The treatment was carried out in a muffle furnace at a temperature of 750°C in an atmosphere of neutral gas (N2). The mixture was rapidly heated to 700°C, and then the temperature was raised to 750°C at a rate of 10°C/min. After this temperature was attained, the reaction mixture was held for 30 min, and then it was cooled to ambient temperature. All the time, the neutral gas (N2) was flowing inside the furnace at a rate of 30 L/min. When the reaction mixture reached ambient temperature, it was neutralised with 5% HCl solution. The carbon modified in this way gave the solution a green colour that remained during the initial period of washing. After each subsequent wash out of the potassium base, the suspension was decanted, diluted with distilled water, and its pH value was measured. This treatment was repeated several times, until the pH of the filtrate reached 6.5. When the specified pH was achieved, the active carbon was separated from the solution by filtration under reduced pressure of 10–15 mmHg, rinsing the filter cake with distilled water, which was then dried at a temperature of 120°C. The modified product was obtained with a yield of 60.5% (m/m). The KOH modified active carbon was denoted by Picazine K.

3. Evaluation of Properties Active Carbon and Product of Reactivation

3.1. Sieve Analysis

In order to determine the size distribution of the particles of both active carbons, size analysis was performed [7] for both active carbons (Figure 1).

The results, and the calculated values of the equivalent diameter, prove that Picazine carbon undergoes far-reaching disintegration as a result of high-temperature KOH treatment, and the product obtained shows two predominant particle sizes (ca. 0.2 and 0.7 mm). A change in the particle size of the active carbons, as well as the modification itself, significantly affects the values of different kind of densities.

3.2. Densities Measurements

Important properties of adsorbents are their densities: bulk density (), apparent density (), and real density (). Bulk density was determined by Powder Characteristics Tester [8], apparent density was determined by using mercury displacement, and real density was determined by GeoPyc 1330 Envelope Density Analyzer [9].

Pore volumes () for both carbons were calculated from and using the following equation:

Total porosity () that includes the volume of interparticle space and the volume present inside adsorbent particles was determined from the following relation:

The results of density determination and the values calculated from (1) and (2) are given in Table 1.

PropertiesPicazinePicazine K

Bulk density (), g/cm30.2040.120
Apparent density (), g/cm30.4500.325
Real density (), g/cm31.7772.669
Pore volume (), cm3/cm31.6602.702
Total porosity (), cm3/cm30.8850.995

It is clear from Table 1 that the reduction of potassium hydroxide to metallic potassium [10] may cause an increase in for Picazine K, and, in this way, affect the value of the pore volume and total porosity.

The porous structure of the carbons was analysed by low-temperature nitrogen adsorption. Adsorption-desorption isotherms were determined using ASAP 2020 Micromeritics instrument. The measurements were carried out at 77 K in the pressure range of 0.00001–0.999. Both active carbon isotherms are shown in Figure 2.

The volume of micropores (), characteristic energy of adsorption (), and surface area micropores () were determined according to Dubinin-Radushkevich equation [11], mesopores surface area () and volume mesopores () were determined by BJH method [12], and the specific surface was obtained using the BET equation. The results are summarized in Table 2.

Active carbonPicazinePicazine K

BET surface area, m2/g14622939
Total pore volume, cm3/g, 1.0241.488
Micropore volume, , cm3/g0.4941.001
Energy of adsorption, , kJ/kmol16.2217.77
Surface area micropores, , m2/g13922817
Mesopores surface area, , m2/g (BHJ)22688
Volume mesopores, , cm3/g (BHJ)0.2880.089

The treatment of Picazine carbon with potassium hydroxide caused increase in its structural parameters. The highest increase was found in the case of micropores, surface area, and total pore volume. In consequence, the volume of mesopores decreases, so did their surface area. The increase in the characteristic adsorption energy is mainly due to the narrowing of micropore size as a result of KOH reactivation. Using calculations micropore size by McEnaney equation [13] it was found that, for adsorption energy , size micropores amount to 0.40 nm, and, for , size equals 0.36 nm in slit pore model.

The adsorbent obtained has significantly better structural properties than the initial active carbon.

3.3. Adsorption of Methane and Carbon Dioxide

For both active carbons, methane and carbon dioxide adsorption isotherms were determined using the volumetric method at a pressure of up to 3 MPa using an original measuring apparatus [14]. The measurement principle consisted in the expansion of a gas of known pressure and volume from the dosing space into the adsorbent containing ampoule. Figure 3 shows the apparatus for studying sorption and desorption gases under elevated pressures.

The determination of the so-called excess isotherms was carried out at 25°C. The molar volume of the gas for a given pressure and temperature was calculated using the Beattie-Bridgeman equation that well describes the state of methane and carbon dioxide in the studied pressure and temperature range [15].

Figure 4 presents excess adsorption isotherms of methane and carbon dioxide on the original and modified Picazine.

Treating Picazine carbon with potassium hydroxide nearly doubled the adsorption capacity for CH4 and CO2, as calculated from 3.0 MPa isotherms.

From the technical point of view, the purpose of Picazine K carbon in the pressure range 0–1.0 MPa may be CO2 separation from the biogas using the PSA method and coalmine gas or nitrogen-containing natural gas enrichment with methane.

At a pressure of 3 MPa and beyond, additionally activated carbons may found application for storage of fuels and sequestration of CO2 [16].

4. Conclusions

A significant increase in the adsorption capacity of Picazine active carbon, an active carbon manufactured on an industrial scale from wood, results from additional potassium hydroxide chemical activation.

The carbon thus obtained possesses nearly double the adsorption capacity for methane and carbon dioxide. The porous structure parameters of the active carbon determined prior to and after the modification process correlate very well with the high-pressure adsorption values for both gases.

The product of the reactivation may be used for instance for gaseous fuel storage and for separation of nonliquefying gases using the PSA method.

Conflict of Interests

The author declares that there is no conflict of interests regarding the publication of this paper.


The author is grateful to the AGH University of Science and Technology (Project no. for the financial support of the research described in this paper.


  1. F. Derbyshire, M. Jagtoyen, and M. Thwaites, “Activated carbon-production and applications,” in Porosity in Carbons, J. W. Patrick, Ed., pp. 228–239, Edward Arnolds, London, UK, 1995. View at: Google Scholar
  2. W. Tongpoothorn, M. Sriuttha, P. Homchan, S. Chanthai, and C. Ruangviriyachai, “Preparation of activated carbon derived from Jatropha curcas fruit shell by simple thermo-chemical activation and characterization of their physico-chemical properties,” Chemical Engineering Research and Design, vol. 89, no. 3, pp. 335–340, 2011. View at: Publisher Site | Google Scholar
  3. P. Kleszyk, P. Ratajczak, P. Skowron et al., “Carbons with narrow pore size distribution prepared by simultaneous carbonization and self-activation of tobacco stems and their application to supercapacitors,” Carbon, vol. 81, no. 1, pp. 148–157, 2015. View at: Publisher Site | Google Scholar
  4. F. Derbyshire, M. Jagtoyen, R. Andrews, A. Rao, I. Martin-Gullón, and E. A. Grulke, “Carbon materials in environmental applications,” Chemistry and Physics of Carbon, vol. 27, pp. 1–66, 2000. View at: Google Scholar
  5. B. Buczek and E. Wolak, “Potassium hydroxide modified active carbon for adsorptive refrigerators,” Adsorption, vol. 14, no. 2-3, pp. 283–287, 2008. View at: Publisher Site | Google Scholar
  6. A. Perrin, A. Celzard, J. F. Marêché, and G. Furdin, “Improved methane storage capacities by sorption on wet active carbons,” Carbon, vol. 42, no. 7, pp. 1243–1249, 2004. View at: Publisher Site | Google Scholar
  7. T. Allen, Particle Size Measurement, Chapman and Hall, London, UK, 1984.
  8. B. Buczek and E. Vogt, “An experimental procedure and apparatuses for measurement of density of density of porous particles,” in Characterisation of Porous Solids III, Studies in Surface Science and Catalysis, J. Rouquerol, F. Rodriguez-Reinoso, K. S. W. Sing, and K. K. Unger, Eds., vol. 87, pp. 339–344, Elsevier, Amsterdam, The Netherlands, 1994. View at: Google Scholar
  9. P. Webb and C. Orr, Analytical Methods in Fine Particle Technology, Micromeritics Instrument, Norcross, Ga, USA, 1997.
  10. Y. Otowa, Y. Nojima, and M. Itoh, Activation Mechanism, Surface Properties and Adsorption Characteristics of Koh Activated High Surface Area, Fundamentals of Adsorption, Kluwer Academic, Boston, Mass, USA, 1996.
  11. M. M. Dubinin, “Adsorption properties and microporous structures of carbonaceous adsorbents,” Carbon, vol. 25, no. 5, pp. 593–598, 1987. View at: Publisher Site | Google Scholar
  12. E. P. Barrett, L. G. Joyner, and P. P. Halenda, “The determination of pore volume and area distributions in porous substances. I. Computations from nitrogen isotherms,” Journal of the American Chemical Society, vol. 73, no. 1, pp. 373–380, 1951. View at: Publisher Site | Google Scholar
  13. B. McEnaney, “Estimation of the dimensions of micropores in active carbons using the Dubinin-Radushkevich equation,” Carbon, vol. 25, no. 1, pp. 69–75, 1987. View at: Publisher Site | Google Scholar
  14. A. Nodzeński, “Sorption and desorption of gases (CH4, CO2) on hard coal and active carbon at elevated pressures,” Fuel, vol. 77, no. 11, pp. 1243–1246, 1998. View at: Publisher Site | Google Scholar
  15. R. C. Reid and T. K. Sherwood, The Properties of Gases and Liquids, McGraw-Hill, New York, NY, USA, 1974.
  16. D. Damiani, J. T. Litynski, H. G. McIlvried, D. M. Vikara, and R. D. Srivastava, “The US Department of Energy's R&D program to reduce greenhouse gas emissions through beneficial uses of carbon dioxide,” Greenhouse Gases: Science and Technology, vol. 2, no. 1, pp. 9–19, 2012. View at: Publisher Site | Google Scholar

Copyright © 2016 Bronislaw Buczek. This is an open access article distributed under the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited.

Related articles

No related content is available yet for this article.
 PDF Download Citation Citation
 Download other formatsMore
 Order printed copiesOrder

Related articles

No related content is available yet for this article.

Article of the Year Award: Outstanding research contributions of 2021, as selected by our Chief Editors. Read the winning articles.